EP3693377A4 - Verfahren zur herstellung einer peptidverbindung - Google Patents

Verfahren zur herstellung einer peptidverbindung Download PDF

Info

Publication number
EP3693377A4
EP3693377A4 EP18864861.2A EP18864861A EP3693377A4 EP 3693377 A4 EP3693377 A4 EP 3693377A4 EP 18864861 A EP18864861 A EP 18864861A EP 3693377 A4 EP3693377 A4 EP 3693377A4
Authority
EP
European Patent Office
Prior art keywords
peptide compound
producing peptide
producing
compound
peptide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP18864861.2A
Other languages
English (en)
French (fr)
Other versions
EP3693377A1 (de
Inventor
Akihiro Nagaya
Michiharu HANDA
Naohiko Yasuda
Madoka Yoshino
Yutaka Kobayashi
Keiichi Masuya
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nissan Chemical Corp
Peptidream Inc
Original Assignee
Nissan Chemical Corp
Peptidream Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nissan Chemical Corp, Peptidream Inc filed Critical Nissan Chemical Corp
Publication of EP3693377A1 publication Critical patent/EP3693377A1/de
Publication of EP3693377A4 publication Critical patent/EP3693377A4/de
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
    • C07K1/061—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
    • C07K1/063—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups for alpha-amino functions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/02—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length in solution
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
    • C07K1/061—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
    • C07K1/062—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups for alpha- or omega-carboxy functions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0802—Tripeptides with the first amino acid being neutral
    • C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10—Tetrapeptides
    • C07K5/1002—Tetrapeptides with the first amino acid being neutral
    • C07K5/1016—Tetrapeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
EP18864861.2A 2017-10-03 2018-10-03 Verfahren zur herstellung einer peptidverbindung Pending EP3693377A4 (de)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2017193309 2017-10-03
JP2018134575 2018-07-17
JP2018180501 2018-09-26
PCT/JP2018/037032 WO2019069978A1 (ja) 2017-10-03 2018-10-03 ペプチド化合物の製造方法

Publications (2)

Publication Number Publication Date
EP3693377A1 EP3693377A1 (de) 2020-08-12
EP3693377A4 true EP3693377A4 (de) 2021-06-30

Family

ID=65995128

Family Applications (1)

Application Number Title Priority Date Filing Date
EP18864861.2A Pending EP3693377A4 (de) 2017-10-03 2018-10-03 Verfahren zur herstellung einer peptidverbindung

Country Status (7)

Country Link
US (1) US20200291061A1 (de)
EP (1) EP3693377A4 (de)
JP (1) JP7196087B2 (de)
CN (1) CN111164092B (de)
CA (1) CA3078393A1 (de)
TW (1) TWI811246B (de)
WO (1) WO2019069978A1 (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3960751A4 (de) * 2019-04-25 2023-01-11 Nissan Chemical Corporation Verfahren zur herstellung einer glycosidverbindung
EP3960725A4 (de) * 2019-04-26 2023-05-03 Nissan Chemical Corporation Verfahren zur herstellung einer triorganosilanverbindung
JP7143819B2 (ja) * 2019-06-05 2022-09-29 信越化学工業株式会社 嵩高い置換基を有するオルガノシラン化合物およびその製造方法
CN114206901B (zh) * 2019-08-30 2024-02-20 日产化学株式会社 肽化合物的制造方法
US20230037643A1 (en) * 2019-12-23 2023-02-09 Otsuka Chemical Co., Ltd. Method for producing peptide
US20240182517A1 (en) * 2021-03-09 2024-06-06 Chubu University Educational Foundation Silane-containing condensed cyclic dipeptide compound, production method therefor, and method for producing polypeptide compound using same
WO2023136301A1 (ja) * 2022-01-17 2023-07-20 学校法人中部大学 ペプチド化合物の製造方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993005065A1 (en) * 1991-08-30 1993-03-18 Porton Developments Limited Preparation of peptides by a solid-phase synthesis and intermediates therefor
WO2012087888A2 (en) * 2010-12-22 2012-06-28 Onyx Pharmaceuticals, Inc. Efficient peptide couplings and their use in the synthesis and isolation of a cyclopenta (g) quinazoline trisodium salt

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8827083D0 (en) 1988-11-19 1988-12-21 Porton Prod Ltd Trialkylsilyl esters of amino acids & their use in synthesis of peptides
NZ610301A (en) * 2007-01-30 2015-03-27 Bp Corp North America Inc Enzymes for the treatment of lignocellulosics, nucleic acids encoding them and methods for making and using them
CN101279998B (zh) * 2008-05-13 2011-07-06 吉尔生化（上海）有限公司 一种c-端乙胺化多肽及其衍生物的制备方法
WO2010103857A1 (ja) * 2009-03-12 2010-09-16 国立大学法人北海道大学 ケイ素含有保護基を用いた糖ペプチド固相合成方法および合成装置
JP6011528B2 (ja) * 2011-05-31 2016-10-19 味の素株式会社 ペプチドの製造方法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993005065A1 (en) * 1991-08-30 1993-03-18 Porton Developments Limited Preparation of peptides by a solid-phase synthesis and intermediates therefor
WO2012087888A2 (en) * 2010-12-22 2012-06-28 Onyx Pharmaceuticals, Inc. Efficient peptide couplings and their use in the synthesis and isolation of a cyclopenta (g) quinazoline trisodium salt

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
BORSUK K ET AL: "Application of substituted 2-(trimethylsilyl)ethyl esters to suppress diketopiperazine formation", TETRAHEDRON LETTERS, ELSEVIER, AMSTERDAM , NL, vol. 45, no. 18, 26 April 2004 (2004-04-26), pages 3585 - 3588, XP027092766, ISSN: 0040-4039, [retrieved on 20040409] *
MARCO BRANDSTÄTTER ET AL: "Synthesis of 2-Oxazolines by in Situ Desilylation and Cyclodehydration of [beta]-Hydroxyamides", JOURNAL OF ORGANIC CHEMISTRY, vol. 80, no. 1, 18 December 2014 (2014-12-18), Washington, pages 40 - 51, XP055590110, ISSN: 0022-3263, DOI: 10.1021/jo5016695 *
MARTIN STRACK ET AL: "Silyl-Based Alkyne-Modifying Linker for the Preparation of C-Terminal Acetylene-Derivatized Protected Peptides", JOURNAL OF ORGANIC CHEMISTRY, vol. 77, no. 22, 1 November 2012 (2012-11-01), Washington, pages 9954 - 9958, XP055590113, ISSN: 0022-3263, DOI: 10.1021/jo302305d *

Also Published As

Publication number Publication date
WO2019069978A1 (ja) 2019-04-11
JPWO2019069978A1 (ja) 2020-11-05
TWI811246B (zh) 2023-08-11
EP3693377A1 (de) 2020-08-12
US20200291061A1 (en) 2020-09-17
TW201922769A (zh) 2019-06-16
CN111164092A (zh) 2020-05-15
CA3078393A1 (en) 2019-04-11
JP7196087B2 (ja) 2022-12-26
CN111164092B (zh) 2023-12-26

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